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61.
In this article, we have studied the bound anionic states of DNA and RNA nucleobases using the newly developed bt-PNO-EOM-CCSD method and extended basis sets. All of the five nucleobases have a single bound anionic state, which is dipole bound in nature. The electron affinity corresponding to the dipole-bound state is found to be extremely sensitive to the used basis set, and a proper agreement with the available experimental data requires a large basis set with a sufficient number of diffuse functions. Electron correlation plays a major role in stabilizing the bound anionic states of nucleobases. No valence-bound anionic states are observed for any of the nucleobases. 相似文献
62.
Divya Iyer Vaqar M. S. Syed Samanvaya Srivastava 《Journal of polymer science. Part A, Polymer chemistry》2021,59(22):2895-2904
The addition of monovalent salts to polyelectrolyte complexes (PECs) comprising oppositely charged polyelectrolytes results in diminishing propensity for complexation, leading to complexes with higher water contents and lower moduli. However, the corresponding influence of multivalent ions on polyelectrolyte complexation has not yet been explored beyond enhanced screening effects. Here, we elucidate the significant impact of the valency of the salt cation on the composition, ion partitioning, and viscoelasticity of charge-matched PECs comprising sodium salt of poly(acrylic acid) and poly(allylamine hydrochloride). Notably, preferential partitioning of divalent cations (Ca2+ and Sr2+) into the complexes is observed, in stark contrast to the depletion of monovalent ions (Na+) from the complexes. Concomitantly, electrostatic bridging of polyanion chains by divalent ions is found to hinder their relaxation, manifesting as a non-monotonic evolution of the shear moduli of the complexes with increasing divalent salt concentrations. Relatedly, a failure of time-salt and time-ionic strength superposition approaches in presence of divalent ions is demonstrated, highlighting the nontrivial influence of these ions on chain relaxation behavior. 相似文献
63.
An efficacious synthesis of N-1–, C-3–substituted indole derivatives and their antimicrobial studies
A novel series of 11 C-3– and N-1–substituted oxoacetamide indole derivatives were synthesized by reacting with various aromatic amines and alkyl halides. These compounds were characterized by using various spectral techniques, ie, 1HNMR, 1HNMR-D2O, 13CNMR, UV, elemental analysis, IR, and mass spectrometery. In vitro, antimicrobial studies of resultant compounds were carried out against two bacterial strains, Pseudomonas aeruginosa and Pseudomonas oryzihabitans using disc plate method. All the tested compounds showed vital efficiency as antimicrobial agents against both the bacterial strains. The results revealed that synthesized indole derivative 2-(1-(3-bromopropyl)-1H-indol-3-yl)-N-(2-nitrophenyl)-2-oxoacetamide displayed the best antimicrobial activity as compared with all other synthesized compounds. 相似文献
64.
Sonali P. D. Bhade P. J. Reddy S. Anilkumar R. K. Singhal D. D. Rao 《Journal of Radioanalytical and Nuclear Chemistry》2018,315(1):13-20
Liquid scintillation alpha beta discrimination technique based on pulse shape analysis (PSA) was evaluated for determination of 226Ra and 222Rn in water samples. In view of the significance of calibration, for the reliable and precise determination of 226Ra and 222Rn concentrations in water samples, calibration procedures were standardized for single and two phase systems using Quantulus 1220 liquid scintillation counter. PSA optimization and efficiency calibrations were performed using 226Ra standard rather than conventionally used pure alpha and beta standards and substantiated by measuring the activity concentrations of 226Ra and 222Rn in the spiked water samples. 相似文献
65.
66.
o-Methyl-substituted Me-IBX is the first modified analog of IBX that oxidizes alcohols in common organic solvents at room temperature, due to a composite of two factors, that is, low solubility and hypervalent twisting-promoted rate enhancement. Furthermore, the reagent is efficient for selective oxidation of sulfides to sulfoxides, a transformation that otherwise occurs only sluggishly with standard IBX. The facile synthetic accessibility and its mild as well as non-hazardous nature render Me-IBX a stable equivalent of Dess-Martin periodinane reagent in organic oxidations. 相似文献
67.
68.
A mathematical model has been developed that could predict kinetic parameters for the adsorption of divalent cations (lead, copper and zinc) onto low-grade rock phosphate using experimental data. The experiments were conducted with the initial concentrations of metal ions ranging from 10 to 100 mg/L. The mathematical model is based on application of Freundlich isotherm to mass transfer across the film surrounding the adsorbent. A code in C programming is used to numerically integrate the model equation, and to obtain the best simulated values of Freundlich constants K, N, order of reaction n, and film transfer coefficient, alpha. It is observed that the adsorption of metal ions on rock phosphate is more sensitive to N,n, and alpha in comparison to K, and lead is adsorbed more favorably than copper and zinc. 相似文献
69.
Ahuja R Singhal NK Ramanujam B Ravikumar M Rao CP 《The Journal of organic chemistry》2007,72(9):3430-3442
A galactosyl-naphthyl-imine-based derivative, 1-(beta-D-galactopyranosyl-1'-deoxy-1'-iminomethyl)-2-hydroxynaphthalene (GNI), and a galactosyl-naphthyl-amine-based derivative, 1-(galactopyranosyl-1'-deoxy-1'-aminomethyl)-2-hydroxynaphthalene (GNA), possessing an ONO binding core were studied for their recognition of naturally occurring amino acids using fluorescence and absorption spectroscopy, and the corresponding association constants were derived for the complexes formed. The complexes formed between GNI/GNA and amino acids were supported by electrospray ionization mass spectrometry (ESI/MS). The structures of the complexes were optimized by computational studies using density functional theory, and stabilization energies were computed for the complexes to substantiate the interactions present between GNI/GNA and amino acid. The interactions were found to be primarily hydrogen bonding in nature. These interactions are reminiscent of those present in the lectin-carbohydrate and glycosidase substrate. Thus, the carbohydrate moiety present in GNI shows high specificity toward the -COOH group of the amino acid, which may be relevant to such interactions present between the carbohydrates and the polypeptides. 相似文献
70.
The trace element Zn in the Zn-doped multi-layer ш - V group compound semiconductor was detected by means of Resonant Laser Ablation/lomzation(RLA). A detection limit of 2. 5 X 1017 atoms/cm3 (about 5 ppm) has been estimated. The mass spectra and the optical resonant ionization spectrum around 214 nm are given in this paper. 相似文献